StatLock¿ IV Premium Catheter Stabilization Device — Class II medical device recall Z-2120-2017
Terminated recall by Bard Access Systems Inc., reported 2017-05-31, distributed nationwide. StatLockTM IV Premium Catheter Stabilization Device may contain an incorrectly sized retainer clip.
| Recall number | Z-2120-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Bard Access Systems Inc., Salt Lake City, UT, United States |
| Recall initiated | 2017-04-25 |
| Classified | 2017-05-19 |
| Reported by FDA | 2017-05-31 |
| Terminated | 2017-08-21 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA |
| Quantity | 4,500 units |
| Lot numbers | JUAQF675 |
| Expiration dates | 2019-02-28 |
Product
StatLock¿ IV Premium Catheter Stabilization Device, product code IV0570. sterile. Packaging: packaged as single units in tyvek to film pouches, the product is distributed in cartons containing 25 devices and cases containing 250 devices.
Reason for recall
StatLockTM IV Premium Catheter Stabilization Device may contain an incorrectly sized retainer clip.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2120-2017. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.